CAS 1227476-98-3

Benzenepropanamide, α-[(5-chloro-2-hydroxybenzoyl)amino]-N-(4-chlorophenyl)-, (αR)-

Description:

Benzenepropanamide, α-[(5-chloro-2-hydroxybenzoyl)amino]-N-(4-chlorophenyl)-, (αR)- is a chemical compound characterized by its complex structure, which includes a benzene ring, an amide functional group, and multiple chlorinated aromatic components. The presence of the chloro and hydroxy groups suggests that this compound may exhibit significant biological activity, potentially influencing its solubility and reactivity. The amide linkage indicates that it may participate in hydrogen bonding, which can affect its interaction with biological targets. The stereochemistry denoted by (αR)- implies a specific spatial arrangement of atoms, which can be crucial for its pharmacological properties. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential interactions with biological systems. Additionally, the presence of multiple aromatic rings may contribute to its stability and lipophilicity, influencing its absorption and distribution in biological contexts. Overall, this compound's unique structural features suggest a range of possible applications and biological implications.

Formula: C₂₂H₁₈Cl₂N₂O₃

Synonyms:

• Compound 6k
• MDK-6983
• MDK-6983, 10 mM in DMSO
• MDK6983
• Autophagy inhibitor 6k
• MDK 6983
• Benzenepropanamide, α-[(5-chloro-2-hydroxybenzoyl)amino]-N-(4-chlorophenyl)-, (αR)-
• Autophagy-IN-3

MDK-6983

CAS: 1227476-98-3

MDK-6983

Purity: ≥95%

Molecular weight: 429.3g/mol

Ref: 54-BUP14294

MDK-6983

CAS: 1227476-98-3

MDK-6983 (MDK-6983) is an inhibitor of autophagy and disrupts the dynamics of actin cytoskeleton in human melanoma cells.

Formula: C₂₂H₁₈Cl₂N₂O₃

Purity: 99.68%

Color and Shape: Solid

Molecular weight: 429.3

Ref: TM-T28001